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Genetic insights into the morphogenesis of inner ear hair cells

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/cm.10092openalex-snapshot

Transient expression of the t‐isoform of plastins/fimbrin in the stereocilia of developing auditory hair cells

inferredcites →https://doi.org/10.1002/cne.10944openalex-snapshot

Correlation of expression of the actin filament‐bundling protein espin with stereociliary bundle formation in the developing inner ear

inferredcites →https://doi.org/10.1002/cne.903250208openalex-snapshot

Distribution of the 275 kD hair cell antigen and cell surface specialisations on auditory and vestibular hair bundles in the chicken inner ear

inferredcites →https://doi.org/10.1002/cne.903500204openalex-snapshot

Postnatal development of the hamster cochlea. II. Growth and differentiation of stereocilia bundles

inferredcites →https://doi.org/10.1006/dbio.1999.9424openalex-snapshot

Role of Myosin VI in the Differentiation of Cochlear Hair Cells

inferredcites →https://doi.org/10.1006/geno.1999.6058openalex-snapshot

A New Locus for Late-Onset, Progressive, Hereditary Hearing Loss DFNA20 Maps to 17q25

inferredcites →https://doi.org/10.1007/bf00455401openalex-snapshot

Vestibular hair cell pathology in the Shaker-2 mouse

inferredcites →https://doi.org/10.1007/bf00712112openalex-snapshot

Treadmilling of actin

inferredcites →https://doi.org/10.1007/s000180050426openalex-snapshot

Tails of unconventional myosins

inferredcites →https://doi.org/10.1016/0006-8993(96)00147-3openalex-snapshot

Development of the auditory receptors of the rat: a SEM study

inferredcites →https://doi.org/10.1016/0012-1606(86)90047-3openalex-snapshot

Actin filaments, stereocilia, and hair cells of the bird cochlea

inferredcites →https://doi.org/10.1016/0012-1606(86)90048-5openalex-snapshot

Actin filaments, stereocilia, and hair cells of the bird cochlea

inferredcites →https://doi.org/10.1016/0378-5955(84)90041-8openalex-snapshot

Cross-links between stereocilia in the guinea pig organ of Corti, and their possible relation to sensory transduction

inferredcites →https://doi.org/10.1016/0378-5955(85)90010-3openalex-snapshot

Cross-links between stereocilia in the guinea pig cochlea

inferredcites →https://doi.org/10.1016/0378-5955(86)90077-8openalex-snapshot

Functional organization of the cytoskeleton

inferredcites →https://doi.org/10.1016/0378-5955(89)90059-2openalex-snapshot

The responses of cochlear hair cells to tonic displacements of the sensory hair bundle

inferredcites →https://doi.org/10.1016/0378-5955(91)90027-7openalex-snapshot

Stereociliary bundles reorient during hair cell development and regeneration in the chick cochlea

inferredcites →https://doi.org/10.1016/0378-5955(91)90116-qopenalex-snapshot

The development of links between stereocilia in hair cells of the chick basilar papilla

inferredcites →https://doi.org/10.1016/0378-5955(92)90152-dopenalex-snapshot

Actin-binding and microtubule-associated proteins in the organ of Corti

inferredcites →https://doi.org/10.1016/0378-5955(95)00088-lopenalex-snapshot

Fimbrin expression in the developing rat cochlea

inferredcites →https://doi.org/10.1016/0896-6273(91)90343-xopenalex-snapshot

Tip-link integrity and mechanical transduction in vertebrate hair cells

inferredcites →https://doi.org/10.1016/0896-6273(95)90010-1openalex-snapshot

Calcium imaging of single stereocilia in hair cells: Localization of transduction channels at both ends of tip links

inferredcites →https://doi.org/10.1016/j.molmed.2003.09.008openalex-snapshot

Stereocilia: the long and the short of it

inferredcites →https://doi.org/10.1016/s0006-3495(02)75537-9openalex-snapshot

MYO1A (Brush Border Myosin I) Dynamics in the Brush Border of LLC-PK1-CL4 Cells

inferredcites →https://doi.org/10.1016/s0070-2153(03)57011-9openalex-snapshot

Cell Adhesion Molecules during Inner Ear and Hair Cell Development, Including Notch and Its Ligands

inferredcites →https://doi.org/10.1016/s0092-8674(00)00042-8openalex-snapshot

The Deaf Jerker Mouse Has a Mutation in the Gene Encoding the Espin Actin-Bundling Proteins of Hair Cell Stereocilia and Lacks Espins

inferredcites →https://doi.org/10.1016/s0092-8674(04)00211-9openalex-snapshot

The Mechanism of Myosin VI Translocation and Its Load-Induced Anchoring

inferredcites →https://doi.org/10.1016/s0168-9525(02)02770-1openalex-snapshot

Planar cell polarization: do the same mechanisms regulate Drosophila tissue polarity and vertebrate gastrulation?

inferredcites →https://doi.org/10.1016/s0171-9335(99)80013-2openalex-snapshot

2E4 (Kaptin): A novel actin-associated protein from human blood platelets found in lamellipodia and the tips of the stereocilia of the inner ear

inferredcites →https://doi.org/10.1016/s0378-5955(00)00152-0openalex-snapshot

Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer

inferredcites →https://doi.org/10.1016/s0378-5955(00)00168-4openalex-snapshot

Evolution of hearing in vertebrates: the inner ears and processing

inferredcites →https://doi.org/10.1016/s0378-5955(00)00233-1openalex-snapshot

Severe vestibular and auditory impairment in three alleles of Ames waltzer ( av ) mice

inferredcites →https://doi.org/10.1016/s0378-5955(03)00107-2openalex-snapshot

A new spontaneous mutation in the mouse Ames waltzer gene, Pcdh15

inferredcites →https://doi.org/10.1016/s0378-5955(99)00008-8openalex-snapshot

Stereociliary anomaly in the guinea pig: effects of hair bundle rotation on cochlear sensitivity

inferredcites →https://doi.org/10.1016/s0896-6273(00)00102-1openalex-snapshot

A Targeted Deletion in α-Tectorin Reveals that the Tectorial Membrane Is Required for the Gain and Timing of Cochlear Feedback

inferredcites →https://doi.org/10.1016/s0955-0674(99)00059-9openalex-snapshot

Parallel actin bundles and their multiple actin-bundling proteins

inferredcites →https://doi.org/10.1016/s0959-4388(02)00287-8openalex-snapshot

Revisiting cell fate specification in the inner ear

inferredcites →https://doi.org/10.1016/s0960-9822(03)00374-9openalex-snapshot

Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse

inferredcites →https://doi.org/10.1016/s1534-5807(02)00147-8openalex-snapshot

The Atypical Cadherin Flamingo Links Frizzled and Notch Signaling in Planar Polarity Establishment in the Drosophila Eye

inferredcites →https://doi.org/10.1023/a:1007090626294openalex-snapshot

Tailchaser (Tlc): A new mouse mutation affecting hair bundle differentiation and hair cell survival

inferredcites →https://doi.org/10.1023/a:1026515619443openalex-snapshot

Hair cells in the inner ear of the pirouette and shaker 2 mutant mice

inferredcites →https://doi.org/10.1038/281675a0openalex-snapshot

Ionic basis of the receptor potential in a vertebrate hair cell

inferredcites →https://doi.org/10.1038/287291a0openalex-snapshot

Actin in the inner ear: the remarkable structure of the stereocilium

inferredcites →https://doi.org/10.1038/35012009openalex-snapshot

Prestin is the motor protein of cochlear outer hair cells

inferredcites →https://doi.org/10.1038/35038540openalex-snapshot

Sticking together and sorting things out: adhesion as a force in development

inferredcites →https://doi.org/10.1038/374060a0openalex-snapshot

Defective myosin VIIA gene responsible for Usher syndrome type IB

inferredcites →https://doi.org/10.1038/374062a0openalex-snapshot

A type VII myosin encoded by the mouse deafness gene shaker-1

inferredcites →https://doi.org/10.1038/418837aopenalex-snapshot

Rapid renewal of auditory hair bundles

inferredcites →https://doi.org/10.1038/46835openalex-snapshot

Myosin VI is an actin-based motor that moves backwards

inferredcites →https://doi.org/10.1038/78140openalex-snapshot

A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse

inferredcites →https://doi.org/10.1038/79171openalex-snapshot

A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C

inferredcites →https://doi.org/10.1038/79178openalex-snapshot

A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene

inferredcites →https://doi.org/10.1038/83660openalex-snapshot

Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D

inferredcites →https://doi.org/10.1038/83667openalex-snapshot

Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D

inferredcites →https://doi.org/10.1038/83837openalex-snapshot

The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene

inferredcites →https://doi.org/10.1038/nature01059openalex-snapshot

Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier

inferredcites →https://doi.org/10.1038/nature01618openalex-snapshot

Identification of Vangl2 and Scrb1 as planar polarity genes in mammals

inferredcites →https://doi.org/10.1038/nature02483openalex-snapshot

Cadherin 23 is a component of the tip link in hair-cell stereocilia

inferredcites →https://doi.org/10.1038/nature02484openalex-snapshot

Mutations in cadherin 23 affect tip links in zebrafish sensory hair cells

inferredcites →https://doi.org/10.1038/ncb0402-e101openalex-snapshot

Intercellular adhesion, signalling and the cytoskeleton

inferredcites →https://doi.org/10.1038/ng0195-86openalex-snapshot

A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17

inferredcites →https://doi.org/10.1038/ng0598-60openalex-snapshot

Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment

inferredcites →https://doi.org/10.1038/ng1208openalex-snapshot

Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31

inferredcites →https://doi.org/10.1038/ng1295-369openalex-snapshot

The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells

inferredcites →https://doi.org/10.1038/nn1089openalex-snapshot

Fast adaptation of mechanoelectrical transducer channels in mammalian cochlear hair cells

inferredcites →https://doi.org/10.1038/nn1120openalex-snapshot

Developmental acquisition of sensory transduction in hair cells of the mouse inner ear

inferredcites →https://doi.org/10.1038/nrm730openalex-snapshot

Prestin, a new type of motor protein

inferredcites →https://doi.org/10.1046/j.1460-9568.2002.02213.xopenalex-snapshot

A novel stereocilia defect in sensory hair cells of the deaf mouse mutant Tasmanian devil

inferredcites →https://doi.org/10.1073/pnas.0308620100openalex-snapshot

Radixin is a constituent of stereocilia in hair cells

inferredcites →https://doi.org/10.1073/pnas.1030502100openalex-snapshot

Dynamic assembly of surface structures in living cells

inferredcites →https://doi.org/10.1073/pnas.232579599openalex-snapshot

The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions

inferredcites →https://doi.org/10.1073/pnas.2334417100openalex-snapshot

Myosin XVa localizes to the tips of inner ear sensory cell stereocilia and is essential for staircase formation of the hair bundle

inferredcites →https://doi.org/10.1073/pnas.93.26.15469openalex-snapshot

Regeneration of broken tip links and restoration of mechanical transduction in hair cells

inferredcites →https://doi.org/10.1073/pnas.97.22.11736openalex-snapshot

Cochlear mechanisms from a phylogenetic viewpoint

inferredcites →https://doi.org/10.1074/jbc.274.49.34507openalex-snapshot

Cortical Actin Organization: Lessons from ERM (Ezrin/Radixin/Moesin) Proteins

inferredcites →https://doi.org/10.1083/jcb.109.6.2853openalex-snapshot

The structure of the cuticular plate, an in vivo actin gel.

inferredcites →https://doi.org/10.1083/jcb.112.4.641openalex-snapshot

Three different actin filament assemblies occur in every hair cell: each contains a specific actin crosslinking protein.

inferredcites →https://doi.org/10.1083/jcb.137.6.1287openalex-snapshot

Unconventional Myosins in Inner-Ear Sensory Epithelia

inferredcites →https://doi.org/10.1083/jcb.143.1.121openalex-snapshot

Why Are Two Different Cross-linkers Necessary for Actin Bundle Formation In Vivo and What Does Each Cross-link Contribute?

inferredcites →https://doi.org/10.1083/jcb.146.5.1097openalex-snapshot

Regulated Actin Cytoskeleton Assembly at Filopodium Tips Controls Their Extension and Retraction

inferredcites →https://doi.org/10.1083/jcb.148.1.1openalex-snapshot

F-Actin Bundles Are Derivatives of Microvilli: What Does This Tell US about How Bundles Might Form?

inferredcites →https://doi.org/10.1083/jcb.153.5.947openalex-snapshot

An Atomic Model of Actin Filaments Cross-Linked by Fimbrin and Its Implications for Bundle Assembly and Function

inferredcites →https://doi.org/10.1083/jcb.200309093openalex-snapshot

Espin cross-links cause the elongation of microvillus-type parallel actin bundles in vivo

inferredcites →https://doi.org/10.1083/jcb.200310055openalex-snapshot

An actin molecular treadmill and myosins maintain stereocilia functional architecture and self-renewal

inferredcites →https://doi.org/10.1083/jcb.86.1.244openalex-snapshot

The organization of actin filaments in the stereocilia of cochlear hair cells.

inferredcites →https://doi.org/10.1083/jcb.95.1.249openalex-snapshot

Interactions between actin filaments and between actin filaments and membranes in quick-frozen and deeply etched hair cells of the chick ear.

inferredcites →https://doi.org/10.1083/jcb.96.3.822openalex-snapshot

Actin filaments, stereocilia, and hair cells of the bird cochlea. II. Packing of actin filaments in the stereocilia and in the cuticular plate and what happens to the organization when the stereocilia are bent.

inferredcites →https://doi.org/10.1086/316954openalex-snapshot

Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23

inferredcites →https://doi.org/10.1086/321277openalex-snapshot

Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F

inferredcites →https://doi.org/10.1086/323156openalex-snapshot

MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss

inferredcites →https://doi.org/10.1086/375122openalex-snapshot

Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37

inferredcites →https://doi.org/10.1086/379286openalex-snapshot

Mutations in the γ-Actin Gene (ACTG1) Are Associated with Dominant Progressive Deafness (DFNA20/26)

inferredcites →https://doi.org/10.1093/emboj/19.22.6020openalex-snapshot

Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin–catenins complex

inferredcites →https://doi.org/10.1093/emboj/cdf689openalex-snapshot

Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle

inferredcites →https://doi.org/10.1093/hmg/10.16.1709openalex-snapshot

Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F

inferredcites →https://doi.org/10.1093/hmg/12.5.463openalex-snapshot

Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin

inferredcites →https://doi.org/10.1093/hmg/ddg358openalex-snapshot

PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23

inferredcites →https://doi.org/10.1098/rspb.1956.0028openalex-snapshot

The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse

inferredcites →https://doi.org/10.1111/j.1749-6632.1981.tb30854.xopenalex-snapshot

DIRECTIONAL SENSITIVITY OF INDIVIDUAL VERTEBRATE HAIR CELLS TO CONTROLLED DEFLECTION OF THEIR HAIR BUNDLES*

inferredcites →https://doi.org/10.1113/jphysiol.1985.sp015581openalex-snapshot

Mechano‐electrical transduction currents in isolated vestibular hair cells of the chick.

inferredcites →https://doi.org/10.1121/1.381496openalex-snapshot

Postnatal development in the acoustic system of the house mouse in the light of developing masked thresholds

inferredcites →https://doi.org/10.1126/science.1093923openalex-snapshot

Actin Polymerization-Driven Molecular Movement of mDia1 in Living Cells

inferredcites →https://doi.org/10.1126/science.1094291openalex-snapshot

Convergence of Wnt, ß-Catenin, and Cadherin Pathways

inferredcites →https://doi.org/10.1126/science.278.5341.1315openalex-snapshot

Nonsyndromic Deafness DFNA1 Associated with Mutation of a Human Homolog of the Drosophila Gene diaphanous

inferredcites →https://doi.org/10.1126/science.280.5368.1444openalex-snapshot

Correction of Deafness in shaker-2 Mice by an Unconventional Myosin in a BAC Transgene

inferredcites →https://doi.org/10.1126/science.280.5368.1447openalex-snapshot

Association of Unconventional Myosin MYO15 Mutations with Human Nonsyndromic Deafness DFNB3

inferredcites →https://doi.org/10.1126/science.7839150openalex-snapshot

Mammalian Vestibular Hair Cell Regeneration

inferredcites →https://doi.org/10.1126/science.8456284openalex-snapshot

Ultrastructural evidence for hair cell regeneration in the mammalian inner ear

inferredcites →https://doi.org/10.1126/science.8456285openalex-snapshot

Regenerative proliferation in inner ear sensory epithelia from adult guinea pigs and humans

inferredcites →https://doi.org/10.1136/jmg.2003.011973openalex-snapshot

Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI ( MYO6 )

inferredcites →https://doi.org/10.1136/jmg.2004.018523openalex-snapshot

Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction

inferredcites →https://doi.org/10.1136/jmg.40.12.879openalex-snapshot

A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26)

inferredcites →https://doi.org/10.1146/annurev.cb.08.110192.001353openalex-snapshot

Actin Filaments, Stereocilia, and Hair Cells: How Cells Count and Measure

inferredcites →https://doi.org/10.1146/annurev.genom.4.070802.110347openalex-snapshot

Human Nonsyndromic Sensorineural Deafness

inferredcites →https://doi.org/10.1159/000113335openalex-snapshot

Evolution of the Ear and Hearing: Issues and Questions

inferredcites →https://doi.org/10.1242/dev.00114openalex-snapshot

The chickenRaxLgene plays a role in the initiation of photoreceptor differentiation

inferredcites →https://doi.org/10.1242/dev.00448openalex-snapshot

Wnt signaling mediates reorientation of outer hair cell stereociliary bundles in the mammalian cochlea

inferredcites →https://doi.org/10.1242/dev.116.1.213openalex-snapshot

Actin filaments, stereocilia and hair cells of the bird cochlea VI. How the number and arrangement of stereocilia are determined

inferredcites →https://doi.org/10.1242/dev.125.4.557openalex-snapshot

Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells

inferredcites →https://doi.org/10.1242/dev.129.10.2495openalex-snapshot

The role of Math1 in inner ear development: Uncoupling the establishment of the sensory primordium from hair cell fate determination

inferredcites →https://doi.org/10.1242/jcs.110.6.765openalex-snapshot

Sorting of actin isoforms in chicken auditory hair cells

inferredcites →https://doi.org/10.1242/jcs.114.18.3219openalex-snapshot

Mechanism and role of PDZ domains in signaling complex assembly

inferredcites →https://doi.org/10.1523/jneurosci.19-06-02161.1999openalex-snapshot

Immunocytochemical and Morphological Evidence for Intracellular Self-Repair as an Important Contributor to Mammalian Hair Cell Recovery

inferredcites →https://doi.org/10.1523/jneurosci.19-10-03761.1999openalex-snapshot

The Ankle-Link Antigen: an Epitope Sensitive to Calcium Chelation Associated with the Hair-Cell Surface and the Calycal Processes of Photoreceptors

inferredcites →https://doi.org/10.1523/jneurosci.20-24-j0002.2000openalex-snapshot

Expression and Localization of Prestin and the Sugar Transporter GLUT-5 during Development of Electromotility in Cochlear Outer Hair Cells

inferredcites →https://doi.org/10.1523/jneurosci.23-27-09208.2003openalex-snapshot

A Receptor-Like Inositol Lipid Phosphatase Is Required for the Maturation of Developing Cochlear Hair Bundles

inferredcites →https://doi.org/10.1523/jneurosci.23-34-10815.2003openalex-snapshot

Developmental Assembly of Transduction Apparatus in Chick Basilar Papilla

inferredcites →https://doi.org/10.3109/00016488609108624openalex-snapshot

Stereo-kinociliar Bonds in Mammalian Vestibular Organs

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.6620/zs.2020.59-04zenodo-depositor-declared

inferred← citeshttps://doi.org/10.1002/9780470090121.ch10openalex-snapshot

The Ear

inferred← citeshttps://doi.org/10.1002/aelm.202600015openalex-snapshot

From Flexible to Conformable Pressure Sensors: Mechanisms, Materials, and Biomedical Applications

inferred← citeshttps://doi.org/10.1002/ajmg.a.30949openalex-snapshot

A new locus for nonsyndromic deafness DFNB51 maps to chromosome 11p13‐p12

inferred← citeshttps://doi.org/10.1002/ajmg.a.34391openalex-snapshot

Genome‐wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment

inferred← citeshttps://doi.org/10.1002/anbr.202400004openalex-snapshot

Cutting‐Edge Achievements of Inner Ear Drug Delivery Systems

inferred← citeshttps://doi.org/10.1002/ar.a.20297openalex-snapshot

Genetics of hearing loss: Allelism and modifier genes produce a phenotypic continuum

inferred← citeshttps://doi.org/10.1002/bies.20526openalex-snapshot

Planar cell polarity signaling in vertebrates

inferred← citeshttps://doi.org/10.1002/cm.21159openalex-snapshot

CLIC5 stabilizes membrane‐actin filament linkages at the base of hair cell stereocilia in a molecular complex with radixin, taperin, and myosin VI

inferred← citeshttps://doi.org/10.1002/cm.21964openalex-snapshot

Osteocyte Dendrites: How Do They Grow, Mature, and Degenerate in Mineralized Bone?

inferred← citeshttps://doi.org/10.1002/cne.22001openalex-snapshot

Patterns of expression of Bardet‐Biedl syndrome proteins in the mammalian cochlea suggest noncentrosomal functions

inferred← citeshttps://doi.org/10.1002/cne.22456openalex-snapshot

Asymmetric distribution of cadherin 23 and protocadherin 15 in the kinocilial links of avian sensory hair cells

inferred← citeshttps://doi.org/10.1002/cne.23597openalex-snapshot

Staurosporine‐induced collapse of cochlear hair bundles

inferred← citeshttps://doi.org/10.1002/dvdy.21324openalex-snapshot

Apical and lateral cell protrusions interconnect epithelial cells in live Drosophila wing imaginal discs

inferred← citeshttps://doi.org/10.1002/dvdy.21598openalex-snapshot

Morphogenesis of the node and notochord: The cellular basis for the establishment and maintenance of left–right asymmetry in the mouse

inferred← citeshttps://doi.org/10.1002/emmm.201100922openalex-snapshot

microRNAs: the art of silencing in the ear

inferred← citeshttps://doi.org/10.1002/humu.20266openalex-snapshot

Fates of Cdh23/CDH23 with mutations affecting the cytoplasmic region

inferred← citeshttps://doi.org/10.1002/humu.20469openalex-snapshot

Mutations of theRDXgene cause nonsyndromic hearing loss at theDFNB24locus

inferred← citeshttps://doi.org/10.1002/humu.23042openalex-snapshot

Mutational Spectrum ofMYO15Aand the Molecular Mechanisms of DFNB3 Human Deafness

inferred← citeshttps://doi.org/10.1002/jcp.31003openalex-snapshot

RBM24 is required for mouse hair cell development through regulating pre‐mRNA alternative splicing and mRNA stability

inferred← citeshttps://doi.org/10.1002/jez.b.21055openalex-snapshot

Evolutionary origins of vertebrate placodes: insights from developmental studies and from comparisons with other deuterostomes

inferred← citeshttps://doi.org/10.1002/smll.201801145openalex-snapshot

Small‐Scale Biological and Artificial Multidimensional Sensors for 3D Sensing

inferred← citeshttps://doi.org/10.1007/0-387-31706-6_1openalex-snapshot

Vertebrate Hair Cells: Modern and Historic Perspectives

inferred← citeshttps://doi.org/10.1007/0-387-31706-6_3openalex-snapshot

The Structure and Composition of the Stereociliary Bundle of Vertebrate Hair Cells

inferred← citeshttps://doi.org/10.1007/978-0-387-30425-0_12openalex-snapshot

Physiological Acoustics

inferred← citeshttps://doi.org/10.1007/978-1-4020-6519-4_16openalex-snapshot

Myosin XVA

inferred← citeshttps://doi.org/10.1007/978-1-4419-9523-0_9openalex-snapshot

Genes That Influence Susceptibility to Noise-Induced Hearing Loss

inferred← citeshttps://doi.org/10.1007/978-1-4614-1683-8_8openalex-snapshot

Regulatory Mutations in Human Hereditary Deafness

inferred← citeshttps://doi.org/10.1007/978-1-4939-0755-7_12openalex-snapshot

Physiological Acoustics

inferred← citeshttps://doi.org/10.1007/978-1-59745-523-7_22openalex-snapshot

Fluorescence Microscopy Methods in the Study of Protein Structure and Function

inferred← citeshttps://doi.org/10.1007/978-1-61779-510-7_13openalex-snapshot

Examining Planar Cell Polarity in the Mammalian Cochlea

inferred← citeshttps://doi.org/10.1007/978-3-030-38062-5_12openalex-snapshot

Myosins and Disease

inferred← citeshttps://doi.org/10.1007/978-3-030-38062-5_13openalex-snapshot

Myosins and Hearing

inferred← citeshttps://doi.org/10.1007/978-94-007-5808-7_5openalex-snapshot

Primary Cilia and Inner Ear Sensory Epithelia

inferred← citeshttps://doi.org/10.1007/s00018-006-6148-xopenalex-snapshot

Espins and the actin cytoskeleton of hair cell stereocilia and sensory cell microvilli

inferred← citeshttps://doi.org/10.1007/s00018-010-0448-xopenalex-snapshot

Myo1c mutations associated with hearing loss cause defects in the interaction with nucleotide and actin

inferred← citeshttps://doi.org/10.1007/s00439-018-1936-6openalex-snapshot

Knockout of ush2a gene in zebrafish causes hearing impairment and late onset rod-cone dystrophy

inferred← citeshttps://doi.org/10.1007/s10162-017-0634-8openalex-snapshot

Emerging Gene Therapies for Genetic Hearing Loss

inferred← citeshttps://doi.org/10.1007/s11055-026-02009-9openalex-snapshot

Knowledge of the Genetic Causes of Hearing Loss – The Key to Prophylaxis

inferred← citeshttps://doi.org/10.1007/s11684-016-0494-3openalex-snapshot

Loss of liver kinase B1 causes planar polarity defects in cochlear hair cells in mice

inferred← citeshttps://doi.org/10.1007/s11684-018-0638-8openalex-snapshot

Tprn is essential for the integrity of stereociliary rootlet in cochlear hair cells in mice

inferred← citeshttps://doi.org/10.1007/s12041-022-01416-4openalex-snapshot

Imputation of SNPs associated with presbycusis through linkage disequilibrium analysis in the ILDR1 gene

inferred← citeshttps://doi.org/10.1016/b978-0-12-398358-9.00065-3openalex-snapshot

Protection and Repair of Hearing

inferred← citeshttps://doi.org/10.1016/b978-0-12-818422-6.00061-7openalex-snapshot

Protection and repair of hearing

inferred← citeshttps://doi.org/10.1016/b978-0-443-06811-9.10017-xopenalex-snapshot

Development of the Ears and Eyes

inferred← citeshttps://doi.org/10.1016/b978-012370880-9.00012-8openalex-snapshot

Molecular Anatomy of Receptor Cells and Organ of Corti

inferred← citeshttps://doi.org/10.1016/b978-012370880-9.00024-4openalex-snapshot

Hair Cell Transduction and Adaptation: Physiology and Molecular Mechanisms

inferred← citeshttps://doi.org/10.1016/b978-1-4377-0435-8.00007-xopenalex-snapshot

Hearing Impairment

inferred← citeshttps://doi.org/10.1016/bs.ctdb.2025.03.003openalex-snapshot

Lifelong dynamic maintenance of stereocilia bundles in mammalian auditory hair cells

inferred← citeshttps://doi.org/10.1016/j.ajhg.2009.07.017openalex-snapshot

Mutations in LOXHD1, an Evolutionarily Conserved Stereociliary Protein, Disrupt Hair Cell Function in Mice and Cause Progressive Hearing Loss in Humans

inferred← citeshttps://doi.org/10.1016/j.ajhg.2010.11.010openalex-snapshot

Functional Null Mutations of MSRB3 Encoding Methionine Sulfoxide Reductase Are Associated with Human Deafness DFNB74

inferred← citeshttps://doi.org/10.1016/j.ajhg.2010.12.011openalex-snapshot

Loss-of-Function Mutations of ILDR1 Cause Autosomal-Recessive Hearing Impairment DFNB42

inferred← citeshttps://doi.org/10.1016/j.ajpath.2010.11.063openalex-snapshot

Impaired Vibration of Auditory Ossicles in Osteopetrotic Mice

inferred← citeshttps://doi.org/10.1016/j.anl.2014.04.001openalex-snapshot

Mutations of TMC1 cause deafness by disrupting mechanoelectrical transduction

inferred← citeshttps://doi.org/10.1016/j.bbadis.2007.01.007openalex-snapshot

TRPML3 and hearing loss in the varitint-waddler mouse

inferred← citeshttps://doi.org/10.1016/j.bbadis.2016.08.015openalex-snapshot

miR-431 is involved in regulating cochlear function by targeting Eya4

inferred← citeshttps://doi.org/10.1016/j.bbr.2007.07.032openalex-snapshot

Anxiety and otovestibular disorders: Linking behavioral phenotypes in men and mice

inferred← citeshttps://doi.org/10.1016/j.bbrc.2007.11.102openalex-snapshot

Redox-dependent structural ambivalence of the cytoplasmic domain in the inner ear-specific cadherin 23 isoform

inferred← citeshttps://doi.org/10.1016/j.bone.2019.05.024openalex-snapshot

The CaV1.2 L-type calcium channel regulates bone homeostasis in the middle and inner ear

inferred← citeshttps://doi.org/10.1016/j.bpj.2016.04.017openalex-snapshot

Angular Approach Scanning Ion Conductance Microscopy

inferred← citeshttps://doi.org/10.1016/j.brainres.2006.02.062openalex-snapshot

Hair cell development: Commitment through differentiation

inferred← citeshttps://doi.org/10.1016/j.brainres.2009.10.039openalex-snapshot

Protein 4.1 expression in the developing hair cells of the mouse inner ear

inferred← citeshttps://doi.org/10.1016/j.ceb.2004.12.005openalex-snapshot

When size matters: the dynamic regulation of stereocilia lengths

inferred← citeshttps://doi.org/10.1016/j.ceb.2005.11.002openalex-snapshot

The making of filopodia

inferred← citeshttps://doi.org/10.1016/j.cell.2010.03.049openalex-snapshot

Actin-Bundling Protein TRIOBP Forms Resilient Rootlets of Hair Cell Stereocilia Essential for Hearing

inferred← citeshttps://doi.org/10.1016/j.celrep.2012.06.018openalex-snapshot

Transcriptome Analysis of the Planarian Eye Identifies ovo as a Specific Regulator of Eye Regeneration

inferred← citeshttps://doi.org/10.1016/j.celrep.2018.07.087openalex-snapshot

The Actin Nucleator Cobl Is Critical for Centriolar Positioning, Postnatal Planar Cell Polarity Refinement, and Function of the Cochlea

inferred← citeshttps://doi.org/10.1016/j.cub.2021.04.005openalex-snapshot

The many roles of myosins in filopodia, microvilli and stereocilia

inferred← citeshttps://doi.org/10.1016/j.devbrainres.2005.08.008openalex-snapshot

Time course of auditory impairment in mice lacking the electroneutral sodium bicarbonate cotransporter NBC3 (slc4a7)

inferred← citeshttps://doi.org/10.1016/j.heares.2005.05.006openalex-snapshot

Differential distribution of β- and γ-actin in guinea-pig cochlear sensory and supporting cells

inferred← citeshttps://doi.org/10.1016/j.heares.2011.01.011openalex-snapshot

Development of tonotopy in the auditory periphery

inferred← citeshttps://doi.org/10.1016/j.heares.2013.07.006openalex-snapshot

Cytodifferentiation of hair cells during the development of a basal chordate

inferred← citeshttps://doi.org/10.1016/j.heares.2018.12.012openalex-snapshot

Building and repairing the stereocilia cytoskeleton in mammalian auditory hair cells

inferred← citeshttps://doi.org/10.1016/j.ijporl.2014.08.036openalex-snapshot

Genetics of non-syndromic hearing loss in the Middle East

inferred← citeshttps://doi.org/10.1016/j.jbc.2026.113402openalex-snapshot

Hearing loss associated with CDC42 in mice and humans (Takenouchi–Kosaki syndrome): CDC42 and RHOQ synergistically function in cochlear hair cells

inferred← citeshttps://doi.org/10.1016/j.molmed.2005.12.006openalex-snapshot

From deafness genes to hearing mechanisms: harmony and counterpoint

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2010.08.024openalex-snapshot

Phosphatase and tensin homolog deleted on chromosome 10 regulates sensory cell proliferation and differentiation of hair bundles in the mammalian cochlea

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2016.04.038openalex-snapshot

Distinct roles of Eps8 in the maturation of cochlear and vestibular hair cells

inferred← citeshttps://doi.org/10.1016/j.semcdb.2022.02.004openalex-snapshot

Microtubule and auditory function – an underestimated connection

inferred← citeshttps://doi.org/10.1016/j.ydbio.2005.01.015openalex-snapshot

Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development

inferred← citeshttps://doi.org/10.1016/j.ydbio.2005.12.021openalex-snapshot

Differential expression of espin isoforms during epithelial morphogenesis, stereociliogenesis and postnatal maturation in the developing inner ear

inferred← citeshttps://doi.org/10.1016/j.ydbio.2006.03.009openalex-snapshot

Induction and specification of cranial placodes

inferred← citeshttps://doi.org/10.1016/j.ymthe.2005.02.004openalex-snapshot

A Novel Bovine Virus Efficiently Transduces Inner Ear Neuroepithelial Cells

inferred← citeshttps://doi.org/10.1016/s0001-6519(05)78616-7openalex-snapshot

Estudio genético molecular del síndrome de Usher en España

inferred← citeshttps://doi.org/10.1016/s0065-2660(05)55004-1openalex-snapshot

Genetics of Graviperception in Animals

inferred← citeshttps://doi.org/10.1016/s0070-2153(08)00808-9openalex-snapshot

Chapter Eight Primary Cilia in Planar Cell Polarity Regulation of the Inner Ear

inferred← citeshttps://doi.org/10.1021/jasms.5c00436openalex-snapshot

Mass Spectrometry-Based Spatial Imaging of the Cochlea

inferred← citeshttps://doi.org/10.1038/ncb1219openalex-snapshot

Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia

inferred← citeshttps://doi.org/10.1038/ncomms7873openalex-snapshot

Live-cell imaging of actin dynamics reveals mechanisms of stereocilia length regulation in the inner ear

inferred← citeshttps://doi.org/10.1038/ng1644openalex-snapshot

Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates

inferred← citeshttps://doi.org/10.1038/nn.2330openalex-snapshot

Linking genes underlying deafness to hair-bundle development and function

inferred← citeshttps://doi.org/10.1038/s41378-023-00611-2openalex-snapshot

Bioinspired magnetic cilia: from materials to applications

inferred← citeshttps://doi.org/10.1038/s41597-020-0509-4openalex-snapshot

Serial scanning electron microscopy of anti-PKHD1L1 immuno-gold labeled mouse hair cell stereocilia bundles

inferred← citeshttps://doi.org/10.1038/s41598-021-01876-1openalex-snapshot

Comprehensive molecular-genetic analysis of mid-frequency sensorineural hearing loss

inferred← citeshttps://doi.org/10.1038/s42003-021-02224-9openalex-snapshot

The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis

inferred← citeshttps://doi.org/10.1056/nejmoa043899openalex-snapshot

Modification of Human Hearing Loss by Plasma-Membrane Calcium Pump PMCA2

inferred← citeshttps://doi.org/10.1073/pnas.0500760102openalex-snapshot

A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry ( hscy ) mice

inferred← citeshttps://doi.org/10.1073/pnas.0812446106openalex-snapshot

MicroRNAs are essential for development and function of inner ear hair cells in vertebrates

inferred← citeshttps://doi.org/10.1073/pnas.1417420111openalex-snapshot

Reaction–diffusion model of hair-bundle morphogenesis

inferred← citeshttps://doi.org/10.1073/pnas.1619442114openalex-snapshot

Maturation arrest in early postnatal sensory receptors by deletion of the miR-183/96/182 cluster in mouse

inferred← citeshttps://doi.org/10.1073/pnas.2531557123openalex-snapshot

Regulation of Tmem30b-mediated apical membrane homeostasis in auditory outer hair cells is critical for hearing

inferred← citeshttps://doi.org/10.1074/jbc.m109.025668openalex-snapshot

EHD4 and CDH23 Are Interacting Partners in Cochlear Hair Cells

inferred← citeshttps://doi.org/10.1080/00016489.2025.2479632openalex-snapshot

The 133-kDa N-terminal region of myosin XVa is critical for normal structure and function of auditory and hair cells

inferred← citeshttps://doi.org/10.1080/01677063.2017.1359833openalex-snapshot

Light on a sensory interface linking the cerebrospinal fluid to motor circuits in vertebrates

inferred← citeshttps://doi.org/10.1080/15513815.2018.1547336openalex-snapshot

Targeted Mutation Analysis of the SLC26A4, MYO6, PJVK and CDH23 Genes in Iranian Patients with AR Nonsyndromic Hearing Loss

inferred← citeshttps://doi.org/10.1080/21675511.2016.1220469openalex-snapshot

Listen to your gut: Using adhesion to shape the surface of functionally diverse epithelia

inferred← citeshttps://doi.org/10.1083/jcb.200507072openalex-snapshot

Drosophila melanogaster Cad99C, the orthologue of human Usher cadherin PCDH15, regulates the length of microvilli

inferred← citeshttps://doi.org/10.1083/jcb.200608012openalex-snapshot

The nuclear receptor hepatocyte nuclear factor 4α acts as a morphogen to induce the formation of microvilli

inferred← citeshttps://doi.org/10.1086/499164openalex-snapshot

Mutations in TRIOBP, Which Encodes a Putative Cytoskeletal-Organizing Protein, Are Associated with Nonsyndromic Recessive Deafness

inferred← citeshttps://doi.org/10.1089/ars.2017.7175openalex-snapshot

The Role of MicroRNAs in Environmental Risk Factors, Noise-Induced Hearing Loss, and Mental Stress

inferred← citeshttps://doi.org/10.1089/ten.tea.2014.0340openalex-snapshot

Nonviral Reprogramming of Human Wharton's Jelly Cells Reveals Differences Between ATOH1 Homologues

inferred← citeshttps://doi.org/10.1091/mbc.e05-03-0185openalex-snapshot

Actin Filament Bundles inDrosophilaWing Hairs: Hairs and Bristles Use Different Strategies for Assembly

inferred← citeshttps://doi.org/10.1093/hmg/ddi490openalex-snapshot

The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1

inferred← citeshttps://doi.org/10.1093/hmg/ddl205openalex-snapshot

Usher syndrome: molecular links of pathogenesis, proteins and pathways

inferred← citeshttps://doi.org/10.1093/hmg/ddr503openalex-snapshot

Whirlin interacts with espin and modulates its actin-regulatory function: an insight into the mechanism of Usher syndrome type II

inferred← citeshttps://doi.org/10.1093/hmg/ddv398openalex-snapshot

Individual USH2 proteins make distinct contributions to the ankle link complex during development of the mouse cochlear stereociliary bundle

inferred← citeshttps://doi.org/10.1097/00006982-200512001-00016openalex-snapshot

Usher Syndrome Type 1: Genotype–Phenotype Relationships

inferred← citeshttps://doi.org/10.1097/mao.0b013e318278bf1aopenalex-snapshot

RNA Preservation in Decalcified Cochlear Samples

inferred← citeshttps://doi.org/10.1101/2023.07.09.545606openalex-snapshot

Calcium and Integrin-binding protein 2 (CIB2) controls force sensitivity of the mechanotransducer channels in cochlear outer hair cells

inferred← citeshttps://doi.org/10.1101/2024.09.24.614849openalex-snapshot

Rfx3 controls outer hair cell differentiation, maintenance, and hair bundle formation by regulating the expression of Insm1, Ikzf2 , and Triobp genes

inferred← citeshttps://doi.org/10.1109/ucc48980.2020.00050openalex-snapshot

Hearing loss classification via stationary wavelet entropy and genetic algorithm

inferred← citeshttps://doi.org/10.1111/gtc.12131openalex-snapshot

Caprice/ MISP is a novel F ‐actin bundling protein critical for actin‐based cytoskeletal reorganizations

inferred← citeshttps://doi.org/10.1111/j.1365-2443.2007.01046.xopenalex-snapshot

Vlgr1 is required for proper stereocilia maturation of cochlear hair cells

inferred← citeshttps://doi.org/10.1111/j.1399-0004.2009.01209.xopenalex-snapshot

DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2‐q15

inferred← citeshttps://doi.org/10.1111/jcmm.16610openalex-snapshot

How Transmembrane Inner Ear (TMIE) plays role in the auditory system: A mystery to us

inferred← citeshttps://doi.org/10.1111/jfb.12398openalex-snapshot

Identification of a gene set to evaluate the potential effects of loud sounds from seismic surveys on the ears of fishes: a study with Salmo salar

inferred← citeshttps://doi.org/10.1113/jphysiol.2006.118547openalex-snapshot

Auditory mechanotransduction in the absence of functional myosin‐XVa

inferred← citeshttps://doi.org/10.1126/stke.2822005tr14openalex-snapshot

TRP Channels

inferred← citeshttps://doi.org/10.1136/bmjophth-2025-002272openalex-snapshot

Do variants in the CDH23 gene cause non-syndromic retinitis pigmentosa? Dual validation using whole exome sequencing and a zebrafish model

inferred← citeshttps://doi.org/10.1146/annurev-genet-102108-134135openalex-snapshot

Hearing Loss: Mechanisms Revealed by Genetics and Cell Biology

inferred← citeshttps://doi.org/10.1146/annurev.neuro.29.051605.112917openalex-snapshot

The Micromachinery of Mechanotransduction in Hair Cells

inferred← citeshttps://doi.org/10.1152/physiol.00037.2011openalex-snapshot

Structures of Usher Syndrome 1 Proteins and Their Complexes

inferred← citeshttps://doi.org/10.1155/2011/417217openalex-snapshot

An Update on the Genetics of Usher Syndrome

inferred← citeshttps://doi.org/10.1155/2011/764873openalex-snapshot

Retinal Degenerations: Genetics, Mechanisms, and Therapies

inferred← citeshttps://doi.org/10.1167/iovs.06-0108openalex-snapshot

Ames Waltzer Deaf Mice Have Reduced Electroretinogram Amplitudes and Complex Alternative Splicing of Pcdh15 Transcripts

inferred← citeshttps://doi.org/10.1172/jci.insight.128561openalex-snapshot

TRIOBP-5 sculpts stereocilia rootlets and stiffens supporting cells enabling hearing

inferred← citeshttps://doi.org/10.1172/jci60981openalex-snapshot

Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesis

inferred← citeshttps://doi.org/10.1177/1179547619871907openalex-snapshot

Report of a Novel Splicing Mutation in the MYO15A Gene in a Patient With Sensorineural Hearing Loss and Spectrum of the MYO15A Mutations

inferred← citeshttps://doi.org/10.1186/1471-2156-11-68openalex-snapshot

A symphony of inner ear developmental control genes

inferred← citeshttps://doi.org/10.1186/1471-2164-10-127openalex-snapshot

Identifying components of the hair-cell interactome involved in cochlear amplification

inferred← citeshttps://doi.org/10.1242/dev.045138openalex-snapshot

Cochlear outer hair cells undergo an apical circumference remodeling constrained by the hair bundle shape

inferred← citeshttps://doi.org/10.1242/jcs.02424openalex-snapshot

PHR1, an integral membrane protein of the inner ear sensory cells, directly interacts with myosin 1c and myosin VIIa

inferred← citeshttps://doi.org/10.1242/jcs.02636openalex-snapshot

Usher I syndrome: unravelling the mechanisms that underlie the cohesion of the growing hair bundle in inner ear sensory cells

inferred← citeshttps://doi.org/10.1242/jcs.02831openalex-snapshot

Cadherin Cad99C is required for normal microvilli morphology in Drosophila follicle cells

inferred← citeshttps://doi.org/10.1242/jcs.038083openalex-snapshot

Centrosome positioning in vertebrate development

inferred← citeshttps://doi.org/10.1242/jcs.099242openalex-snapshot

Myosin VIIA regulates microvillus morphogenesis and interacts with cadherin Cad99C in Drosophila oogenesis

inferred← citeshttps://doi.org/10.1242/jcs.143602openalex-snapshot

Maintenance of stereocilia and apical junctional complexes by Cdc42 in cochlear hair cells

inferred← citeshttps://doi.org/10.1242/jcs.209924openalex-snapshot

Unconventional myosin VIIA promotes melanoma progression

inferred← citeshttps://doi.org/10.1266/ggs.16-00041openalex-snapshot

A novel missense variant in the DIAPH1 gene in a Korean family with autosomal dominant nonsyndromic hearing loss

inferred← citeshttps://doi.org/10.13023/etd.2018.321openalex-snapshot

Myosin-XVa is Key Molecule in Establishing the Architecture of Mechanosensory Stereocilia Bundles of the Inner Ear Hair Cells

inferred← citeshttps://doi.org/10.13023/etd.2020.410openalex-snapshot

REMODELING IN THE ACTIN CORE OF THE AUDITORY HAIR CELL STEREOCILIA AS A NOVEL COMPONENT OF TEMPORARY NOISE-INDUCED HEARING LOSS

inferred← citeshttps://doi.org/10.13028/pfss-gf44openalex-snapshot

Identification and Characterization of Components of the Intraflagellar transport (IFT) Machinery: a Dissertation

inferred← citeshttps://doi.org/10.1359/jbmr.080812openalex-snapshot

Bisphosphonate Therapy Ameliorates Hearing Loss in Mice Lacking Osteoprotegerin

inferred← citeshttps://doi.org/10.1369/0022155419841013openalex-snapshot

Rho-kinase and PKCα Inhibition Induces Primary Cilia Elongation and Alters the Behavior of Undifferentiated and Differentiated Temperature-sensitive Mouse Cochlear Cells

inferred← citeshttps://doi.org/10.1371/journal.pgen.1001158openalex-snapshot

β-Actin and γ-Actin Are Each Dispensable for Auditory Hair Cell Development But Required for Stereocilia Maintenance

inferred← citeshttps://doi.org/10.1371/journal.pgen.1002032openalex-snapshot

Roles of the Espin Actin-Bundling Proteins in the Morphogenesis and Stabilization of Hair Cell Stereocilia Revealed in CBA/CaJ Congenic Jerker Mice

inferred← citeshttps://doi.org/10.1371/journal.pgen.1002966openalex-snapshot

A Mutation in the Srrm4 Gene Causes Alternative Splicing Defects and Deafness in the Bronx Waltzer Mouse

inferred← citeshttps://doi.org/10.1371/journal.pgen.1003774openalex-snapshot

An Alteration in ELMOD3, an Arl2 GTPase-Activating Protein, Is Associated with Hearing Impairment in Humans

inferred← citeshttps://doi.org/10.1371/journal.pone.0004753openalex-snapshot

Characterization of the Drosophila Ortholog of the Human Usher Syndrome Type 1G Protein Sans

inferred← citeshttps://doi.org/10.1371/journal.pone.0014807openalex-snapshot

Fascin 2b Is a Component of Stereocilia that Lengthens Actin-Based Protrusions

inferred← citeshttps://doi.org/10.1371/journal.pone.0034894openalex-snapshot

Myosin Light-Chain Kinase Is Necessary for Membrane Homeostasis in Cochlear Inner Hair Cells

inferred← citeshttps://doi.org/10.1371/journal.pone.0036074openalex-snapshot

Mutations of the Mouse ELMO Domain Containing 1 Gene (Elmod1) Link Small GTPase Signaling to Actin Cytoskeleton Dynamics in Hair Cell Stereocilia

inferred← citeshttps://doi.org/10.1371/journal.pone.0073276openalex-snapshot

Notch Signaling Limits Supporting Cell Plasticity in the Hair Cell-Damaged Early Postnatal Murine Cochlea

inferred← citeshttps://doi.org/10.1371/journal.pone.0127926openalex-snapshot

A Biophysical Model for the Staircase Geometry of Stereocilia

inferred← citeshttps://doi.org/10.1371/journal.pone.0133522openalex-snapshot

Whole Exome Sequencing Identified MCM2 as a Novel Causative Gene for Autosomal Dominant Nonsyndromic Deafness in a Chinese Family

inferred← citeshttps://doi.org/10.1371/journal.pone.0135841openalex-snapshot

LKB1 Is Required for the Development and Maintenance of Stereocilia in Inner Ear Hair Cells in Mice

inferred← citeshttps://doi.org/10.1387/ijdb.072344mkopenalex-snapshot

Shaping the mammalian auditory sensory organ by the planar cell polarity pathway

inferred← citeshttps://doi.org/10.1387/ijdb.072365lfopenalex-snapshot

Mouse models to study inner ear development and hereditary hearing loss

inferred← citeshttps://doi.org/10.1523/jneurosci.1124-08.2008openalex-snapshot

Aminoglycoside-Induced Phosphatidylserine Externalization in Sensory Hair Cells Is Regionally Restricted, Rapid, and Reversible

inferred← citeshttps://doi.org/10.1523/jneurosci.1280-08.2008openalex-snapshot

Jxc1/Sobp, Encoding a Nuclear Zinc Finger Protein, Is Critical for Cochlear Growth, Cell Fate, and Patterning of the Organ of Corti

inferred← citeshttps://doi.org/10.1523/jneurosci.2166-06.2006openalex-snapshot

The Chloride Intracellular Channel Protein CLIC5 Is Expressed at High Levels in Hair Cell Stereocilia and Is Essential for Normal Inner Ear Function

inferred← citeshttps://doi.org/10.1523/jneurosci.2672-20.2021openalex-snapshot

Nox3-Derived Superoxide in Cochleae Induces Sensorineural Hearing Loss

inferred← citeshttps://doi.org/10.1523/jneurosci.3998-09.2009openalex-snapshot

The Small GTPase Rac1 Regulates Auditory Hair Cell Morphogenesis

inferred← citeshttps://doi.org/10.1523/jneurosci.5083-14.2015openalex-snapshot

Characterization of the Transcriptome of Nascent Hair Cells and Identification of Direct Targets of the Atoh1 Transcription Factor

inferred← citeshttps://doi.org/10.1523/jneurosci.5456-10.2011openalex-snapshot

An RNA Interference-Based Screen of Transcription Factor Genes Identifies Pathways Necessary for Sensory Regeneration in the Avian Inner Ear

inferred← citeshttps://doi.org/10.15252/emmm.201606609openalex-snapshot

Constitutive activation of DIA1 (DIAPH1) via C‐terminal truncation causes human sensorineural hearing loss

inferred← citeshttps://doi.org/10.1529/biophysj.108.143453openalex-snapshot

Protein Localization by Actin Treadmilling and Molecular Motors Regulates Stereocilia Shape and Treadmilling Rate

inferred← citeshttps://doi.org/10.1534/genetics.106.057372openalex-snapshot

Multiple Quantitative Trait Loci Modify Cochlear Hair Cell Degeneration in the Beethoven (Tmc1Bth) Mouse Model of Progressive Hearing Loss DFNA36

inferred← citeshttps://doi.org/10.1538/expanim.59.57openalex-snapshot

Phenotypic and Expression Analysis of a Novel Spontaneous Myosin VI Null Mutant Mouse

inferred← citeshttps://doi.org/10.21007/etd.cghs.2010.0298openalex-snapshot

The Role of Pkd1 in Mouse Inner Ear Hair Cells

inferred← citeshttps://doi.org/10.21203/rs.3.rs-7581092/v1openalex-snapshot

Therapeutic effect optimization and influencing factors of hyperbaric oxygen in the treatment of sudden sensorineural hearing loss

inferred← citeshttps://doi.org/10.21474/ijar01/2436openalex-snapshot

HOW OSTEOPOROSIS IN POSTMENOPAUSAL WOMEN IS RELATED TO HEARING LOSS?

inferred← citeshttps://doi.org/10.21848/audiol.2007.3.2.135openalex-snapshot

The Validation Study of Otoacoustic Emission by the Regulation of Body Temperature in the Mouse Model

inferred← citeshttps://doi.org/10.2741/3056openalex-snapshot

Cochlear molecules and hereditary deafness

inferred← citeshttps://doi.org/10.2741/4046openalex-snapshot

Autosomal recessive nonsyndromic deafness genes: a review

inferred← citeshttps://doi.org/10.31237/osf.io/pzsyvopenalex-snapshot

Hearing health care in Kenya; a regional field study

inferred← citeshttps://doi.org/10.3389/fcell.2021.637011openalex-snapshot

CCDC154 Mutant Caused Abnormal Remodeling of the Otic Capsule and Hearing Loss in Mice

inferred← citeshttps://doi.org/10.3389/fcell.2021.671364openalex-snapshot

N-Terminus of GRXCR2 Interacts With CLIC5 and Is Essential for Auditory Perception

inferred← citeshttps://doi.org/10.3389/fcell.2024.1359207openalex-snapshot

Sensory cells in tunicates: insights into mechanoreceptor evolution

inferred← citeshttps://doi.org/10.3389/fgene.2022.864228openalex-snapshot

Novel Missense and Splice Site Mutations in USH2A, CDH23, PCDH15, and ADGRV1 Are Associated With Usher Syndrome in Lebanon

inferred← citeshttps://doi.org/10.3389/fnmol.2018.00326openalex-snapshot

Deletion of Kncn Does Not Affect Kinocilium and Stereocilia Bundle Morphogenesis and Mechanotransduction in Cochlear Hair Cells

inferred← citeshttps://doi.org/10.3390/antiox13020219openalex-snapshot

NADPH Oxidase 3: Beyond the Inner Ear

inferred← citeshttps://doi.org/10.3390/genes11121474openalex-snapshot

Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss

inferred← citeshttps://doi.org/10.3390/ijms13078171openalex-snapshot

Proteomic Analysis of the Organ of Corti Using Nanoscale Liquid Chromatography Coupled with Tandem Mass Spectrometry

inferred← citeshttps://doi.org/10.3390/ijms22136723openalex-snapshot

Usher Syndrome: Genetics of a Human Ciliopathy

inferred← citeshttps://doi.org/10.3390/molecules23040882openalex-snapshot

Tracing Actin Filament Bundles in Three-Dimensional Electron Tomography Density Maps of Hair Cell Stereocilia

inferred← citeshttps://doi.org/10.3791/2965openalex-snapshot

Investigating Outer Hair Cell Motility with a Combination of External Alternating Electrical Field Stimulation and High-speed Image Analysis

inferred← citeshttps://doi.org/10.3892/ijmm.2014.1634openalex-snapshot

Myosin light chain kinase regulates hearing in mice by influencing the F-actin cytoskeleton of outer hair cells and cochleae

inferred← citeshttps://doi.org/10.3892/mmr.2014.1953openalex-snapshot

Inhibition of Myo6 gene expression by co-expression of a mutant of transcription factor POU4F3 (BRN-3C) in hair cells

inferred← citeshttps://doi.org/10.4061/2011/416450openalex-snapshot

The Sound of Silence: Mouse Models for Hearing Loss

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